Evidence map›Paper›PMID 22927468›Full record

ArticleThe Journal of cell biology2012

Rad53 is essential for a mitochondrial DNA inheritance checkpoint regulating G1 to S progression.

David G Crider, Luis J García-Rodríguez, Pallavi Srivastava, Leonardo Peraza-Reyes, Krishna Upadhyaya, Istvan R Boldogh, Liza A Pon

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. How do yeast sense mitochondrial dysfunction?Microbial cell (Graz, Austria) · 2016
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Metabolic regulation of the cell cycle.Current opinion in cell biology · 2013
    Review
  19. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

David G CriderDepartment of Pathology and Cell Biology, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.
Luis J García-Rodríguez
Pallavi Srivastava
Leonardo Peraza-Reyes
Krishna Upadhyaya
Istvan R Boldogh
Liza A Pon
Columbia University · US

Funding

MITOCHONDRIAL MOTILITY AND INHERITANCER01GM045735 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI PON, LIZA A · 1993 to 2016
$4.2M
Mitochondrial-cytoskeletal interactions and agingR01GM096445 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PON, LIZA A · 2011 to 2014
$1.3M
NIGMS NIH HHS GM096445NIGMS NIH HHS GM45735NIGMS NIH HHS GM45735S1NIGMS NIH HHS R01 GM045735NIGMS NIH HHS R01 GM096445
6 · The paper itself

Abstract

The Chk2-mediated deoxyribonucleic acid (DNA) damage checkpoint pathway is important for mitochondrial DNA (mtDNA) maintenance. We show in this paper that mtDNA itself affects cell cycle progression. Saccharomyces cerevisiae rho(0) cells, which lack mtDNA, were defective in G1- to S-phase progression. Deletion of subunit Va of cytochrome c oxidase, inhibition of F(1)F(0) adenosine triphosphatase, or replacement of all mtDNA-encoded genes with noncoding DNA did not affect G1- to S-phase progression. Thus, the cell cycle progression defect in rho(0) cells is caused by loss of DNA within mitochondria and not loss of respiratory activity or mtDNA-encoded genes. Rad53p, the yeast Chk2 homologue, was required for inhibition of G1- to S-phase progression in rho(0) cells. Pif1p, a DNA helicase and Rad53p target, underwent Rad53p-dependent phosphorylation in rho(0) cells. Thus, loss of mtDNA activated an established checkpoint kinase that inhibited G1- to S-phase progression. These findings support the existence of a Rad53p-regulated checkpoint that regulates G1- to S-phase progression in response to loss of mtDNA.

Indexed as

Genes, cdcAdenosine TriphosphatasesCell Cycle ProteinsCheckpoint Kinase 2DNA DamageDNA, FungalDNA HelicasesDNA, MitochondrialElectron Transport Complex IVG1 PhaseProtein Serine-Threonine KinasesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsS PhaseAdenosine TriphosphatasesCell Cycle ProteinsCheckpoint Kinase 2DNA, FungalDNA HelicasesDNA, MitochondrialElectron Transport Complex IVProtein Serine-Threonine KinasesRAD53 protein, S cerevisiaeSaccharomyces cerevisiae Proteins

Identifiers

PMID22927468
PMCPMC3432762
OpenAlexW2100080790

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.